Variant #0000001554 (NC_000020.11:g.46007337C>T, NM_004994.2:c.-1590C>T (MMP9))

Individual ID 00000332
Chromosome 20
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.46007337C>T
Published as C1562T
Reference Atheer Awad Mehde et al. (2018), dbSNP
DB-ID MMP9_000001 See all 4 reported entries
dbSNP ID rs3918242
Frequency 31/120
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nuur Athirah Binti Mohd Daud
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nuur Athirah Binti Mohd Daud
Date created 2021-01-06 14:59:09 +08:00 (CST)
Date last edited 2021-09-01 12:14:20 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
MMP9 NM_004994.2 +/. - c.-1590C>T - r.(=) p.(=) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000347 DNA PCR MMP9 4 Nuur Athirah Binti Mohd Daud